Canonical Allele Identifier: CA376552782

Gene: RET

Linked Data

• dbSNP Id: rs761596036
• MyVariant Identifiers: chr10:g.43609082C>G (hg19) ; chr10:g.43113634C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113634C>G , CM000672.2:g.43113634C>G	GRCh38
NC_000010.10:g.43609082C>G , CM000672.1:g.43609082C>G	GRCh37
NC_000010.9:g.42929088C>G	NCBI36
NG_007489.1:g.41566C>G , LRG_518:g.41566C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1442C>G	ENSP00000480088.2:p.Pro481Arg
ENST00000683007.1:n.1412C>G
ENST00000683872.1:n.599C>G
ENST00000340058.6:c.1838C>G	ENSP00000344798.4:p.Pro613Arg
ENST00000355710.8:c.1838C>G MANE Select	ENSP00000347942.3:p.Pro613Arg
ENST00000671844.1:c.*432C>G	ENSP00000500541.1:n.*432C>G
ENST00000672389.1:c.*432C>G	ENSP00000500252.1:n.*432C>G
ENST00000340058.5:c.1838C>G	ENSP00000344798.4:p.Pro613Arg
ENST00000355710.7:c.1838C>G	ENSP00000347942.3:p.Pro613Arg
ENST00000498820.5:c.389C>G	ENSP00000419080.1:p.Pro130Arg
ENST00000615310.4:c.1289+2402C>G	ENSP00000480088.1:n.1289+2402C>G
NM_020630.4:c.1838C>G , LRG_518t2:c.1838C>G	NP_065681.1:p.Pro613Arg
NM_020975.4:c.1838C>G , LRG_518t1:c.1838C>G	NP_066124.1:p.Pro613Arg
XM_011540027.1:c.1838C>G	XP_011538329.1:p.Pro613Arg
NM_001355216.1:c.1076C>G	NP_001342145.1:p.Pro359Arg
NM_020630.5:c.1838C>G	NP_065681.1:p.Pro613Arg
NM_020975.5:c.1838C>G	NP_066124.1:p.Pro613Arg
NM_020975.6:c.1838C>G MANE Select	NP_066124.1:p.Pro613Arg
NM_020630.6:c.1838C>G	NP_065681.1:p.Pro613Arg